Regulatory Affairs Coordinator EFA- Contractor Abbott Laboratories

JOB DESCRIPTION:

R and Responsibilities:

Collaborate with business development and marketing to establish appropriate short, medium, and long-term regulatory strategies by integrating new products into Abbott's portfolio. Prepare regulatory plans and ensure their implementation to achieve long-term objectives for products that can be qualified in terms of sales, market share, and profit contributions.

Working closely with the logistics department to organize the delivery of samples intended for recording within the given timeframes.

Collaborate closely with the marketing and medical departments to review and approve promotional materials in accordance with agreed guidelines and within the given deadlines.

Working with the GPRA for the preparation of files for new products, renewals and variations.

Maintain effective communication with partners, distributors and relevant authorities.

Compliance :

To promote Abbott's corporate values.

Qualit :

Ensure compliance with quality procedures (SOPs) and regulatory requirements.

Ensure that the training sessions are carried out as agreed.

Prerequisites for the position:

• Pharmacist, biologist or graduate in process engineering.
• Desired experience in the pharmaceutical field
• Communication: Excellent written and verbal communication skills.
• Computer skills: Advanced computer skills and familiarity with regulatory document management systems.
• Autonomy and teamwork: Ability to work autonomously and as part of a team.
• Pressure management: Ability to work effectively under pressure.
• Proficiency in English.
• Suitable for travel.